Registered Nurse Research Coordinator

Careers With Purpose\n\nSanford Health is one of the largest and fastest-growing not-for-profit health systems in the United States. We're proud to offer many development and advancement opportunities to our nearly 50,000 members of the Sanford Family who are dedicated to the work of health and healing across our broad footprint.\n\nFacility : Sanford Research\nLocation : Fargo, ND\nAddress : 120 8th St S, Fargo, ND 58103, USA\nShift : 8 Hours - Day Shifts\nJob Schedule : Full time\nWeekly Hours : 40.00\nSalary Range : $27.50 - $44.00\n\nDepartment Details\n\nThe Oncology Research team is looking for a Registered Nurse Coordinator!\n\nThis full time position is located at the Broadway Medical building with day time hours Monday through Friday 8 : 00a-4 : 30pm. Daily tasks include coordinating patient visits, educating families on research protocols, and assisting with lab orders, processing, and screenings.\n\nWhat We're Looking For : \n

• Active Registered Nurse\n
• Prior research experience (preferred)\n
• A collaborative, patient-centered mindset\n\nWhat We Offer : \n
• Supportive and team-oriented environment\n
• Opportunities for ongoing learning and professional development\n
• Competitive benefits package\n\nWhy Join Us?\n\nBe part of a positive, mission-driven department that values teamwork, growth, and the difference we make in the lives of families every day.\n\nJob Summary\n\nProvides an opportunity to learn daily and contribute to treatments of the future. Enthusiasm for learning required, along with participation in educating patients, physicians, nurses and other personnel to the research process. Advanced nursing position that involves clinical patient contact, research study coordination and study data management. Must be able to organize complex components of clinical trials, including test ordering, procedure scheduling and insurance pre-authorization for participants, if applicable.\n\nClinical skills that may be required include, but not limited to : patient assessment for adverse events and assistance with, or completion of, study related procedures as detailed in the research protocol (ex : injections, phlebotomy, or infusions), within the applicable state scope of practice.\n\nDemonstrate a desire and ability to strictly adhere to all levels of institutional, state and federal regulations and established research protocols, and the ability to collaborate with physician investigators to ensure safe and compliant investigational treatment or intervention and follow-up.\n\nAttend investigator meetings and coordinate pre-study site visits. Monitor enrollment goals and modify recruitment plan as needed. Ensure the completion of all screening, eligibility and enrollment procedures. Work with pharmacy to dispense study articles and provide subject education.\n\nClarify questions and concerns with the investigator and sponsor regarding enrollment goals, sponsor expectations and study procedures. Review inclusion / exclusion criteria to assure subject eligibility and review with physician investigator. Review study protocol, informed consent form and follow-up procedures with potential study subjects.\n\nSchedule subjects for follow-up visits to review diaries and questionnaires. Ensure appropriate specimen collection, batching and shipping as required. Document and maintain all study-related procedures, processes and events. Document protocol deviations and exemptions and record accurate and timely data. Maintain accurate source documentation for all case report entries and input data for submission.\n\nRequired to use appropriate nursing assessment skills to evaluate patient condition in response to study intervention. Collect data regarding patient condition for review by the physician investigator.\n\nPrepare case report forms and source documents for sponsor review. Abstract data from medical records, clinic, consultation and referral notes for preparation of study forms and flow sheets.\n\nCommunicate effectively with subjects, research team, Institutional Review Board (IRB) and sponsor representatives.\n\nOccasional local travel between sites and student supervision may be required.\n\nQualifications\n\nGraduate from a nationally accredited nursing program preferred, including, but not limited to, Commission on Collegiate Nursing Education (CCNE), Accreditation Commission for Education in Nursing (ACEN), and National League for Nursing Commission for Nursing Education Accreditation (NLN CNEA).\n\nCurrently holds an unencumbered RN license with the State Board of Nursing where the practice of nursing is occurring and / or possess multistate licensure if in a Nurse Licensure Compact (NLC) state. Obtains and subsequently maintains required department specific competencies and certifications.\n\nBenefits\n\nSanford Health offers an attractive benefits package for qualifying full-time and part-time employees. Depending on eligibility, a variety of benefits include health insurance, dental insurance, vision insurance, life insurance, a 401(k) retirement plan, work / life balance benefits, and a generous time off package to maintain a healthy home-work balance. For more information about Total Rewards, visit https : / / sanfordcareers.com / benefits .\n\nSanford is an EEO / AA Employer M / F / Disability / Vet. If you are an individual with a disability and would like to request an accommodation for help with your online application, please call 1-877-673-0854 or send an email to talent@sanfordhealth.org .\n\nSanford Health has a Drug Free Workplace Policy. An accepted offer will require a drug screen and pre-employment background screening as a condition of employment.\n\nReq Number : R-0235461\nJob Function : Research\nFeatured : Yes